JP2759326B2 - Coke production method - Google Patents
Coke production methodInfo
- Publication number
- JP2759326B2 JP2759326B2 JP63271490A JP27149088A JP2759326B2 JP 2759326 B2 JP2759326 B2 JP 2759326B2 JP 63271490 A JP63271490 A JP 63271490A JP 27149088 A JP27149088 A JP 27149088A JP 2759326 B2 JP2759326 B2 JP 2759326B2
- Authority
- JP
- Japan
- Prior art keywords
- coal
- coke
- char
- gas
- reactivity
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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- Coke Industry (AREA)
Description
【発明の詳細な説明】 [産業上の利用分野] 本発明は、コークスの製造方法に関し、更に詳しく
は、強度と塊度とを犠牲にすることなく反応性を向上さ
せたコークスの新規な製造方法に関するものである。Description: TECHNICAL FIELD The present invention relates to a method for producing coke, and more particularly, to a novel method for producing coke with improved reactivity without sacrificing strength and bulk. It is about the method.
[従来の技術] 従来、高反応性コークスの製造方法としては、原料炭
への配合面からすれば低炭化度炭を配合する方法があ
り、他方乾留条件面からすれば比較的炉温を低温とする
方法があって、通常、低炭化度炭としては亜歴青炭又は
褐炭等が用いられるものである。[Prior art] Conventionally, as a method of producing highly reactive coke, there is a method of blending low-carbonity coal from the viewpoint of blending into raw coal, while the furnace temperature is relatively low from the viewpoint of dry distillation conditions. Usually, sub-bituminous coal or lignite is used as the low-carbon coal.
[発明が解決しようとする課題] しかしながら、原料炭へ低炭化度炭をそのまま配合す
る従来の方法によると、得られるコークスは反応性が高
くなる半面、強度と塊度は低下するようになるので、こ
れらの面から必ずしも反応性をそれ程高くはできない、
といった問題点があった。また、乾溜の炉温を低下させ
る従来の方法では、配合炭装入時に炉温がかなり低下す
ることがあり、炉体維持管理面からもある程度の限界が
ある、という問題点があった。[Problems to be Solved by the Invention] However, according to the conventional method of blending low-rank coal into raw coal as it is, the resulting coke has a high reactivity, but the strength and the bulk are reduced. , From these aspects the reactivity can not always be so high,
There was a problem. Further, in the conventional method of lowering the furnace temperature of the dry distillation, there is a problem that the furnace temperature may be considerably lowered at the time of charging coal blending, and there is a certain limit in terms of furnace body maintenance and management.
本発明は、上記の従来の課題を解決し得る、高反応性
コーススの新規な製造方法の提供を目的とする。An object of the present invention is to provide a novel method for producing a highly reactive causse that can solve the above conventional problems.
[課題を解決するための手段] 本発明者らは、かかる目的を達成すべく鋭意研究を進
めた結果、比較的炭化度の低い石炭を原料とし、急速熱
分解によって瞬時に脱揮発分処理を行い、多量の液状生
成物を得る際に、その熱分解残渣として得られるチャー
の諸性状を検討したところ、揮発分が元の石炭に比較し
適度に低くなっており、また、従来チャーと言われるも
のとは形状の異なったカーボンバルーン状の非常に軽
い、気孔に富む炭材となっていることが判明した。そし
て、かかるチャーを原料炭への配合用炭材としたものを
コークス製造の原料とした場合に、コークスの強度と塊
度とを低下させず、反応性(具体的には例えば反応性指
数17以上)を向上させたコークスが製造できることを見
出だして、本発明に到達したものである。[Means for Solving the Problems] The present inventors have conducted intensive studies to achieve such an object, and as a result, using coal having relatively low carbonization as a raw material, the devolatilization treatment was instantaneously performed by rapid pyrolysis. When a large amount of liquid product was obtained, the properties of the char obtained as a pyrolysis residue were examined.As a result, the volatile content was moderately lower than that of the original coal. It was found to be a very light, porous carbonaceous material in the shape of a carbon balloon with a shape different from that of the carbon material. When the char is used as a raw material for coke production, and the char is used as a raw material for coke production, the reactivity and specificity of the coke are not reduced and the reactivity (specifically, for example, a reactivity index of 17) is obtained. The present inventors have found that coke with the above-mentioned improvements can be produced, and have reached the present invention.
すなわち、本発明は、低炭化度炭を原料とし、反応温
度600〜1000℃、反応時間10秒以下の条件下で急速熱分
解によって得られるチャーを、コークスを製造する際の
原料炭への配合用炭材として使用することを特徴とする
高反応性コークスの製造方法を要旨とするものである。That is, the present invention uses a low-carbon coal as a raw material, a char obtained by rapid pyrolysis under conditions of a reaction temperature of 600 to 1000 ° C. and a reaction time of 10 seconds or less, and blends the char into the raw coal when producing coke. SUMMARY OF THE INVENTION The gist of the present invention is a method for producing highly reactive coke, which is used as a carbonaceous material.
[発明の実施の態様] 以下、本発明方法を図面とともに詳細に説明するに、
第1図は、本発明に係るコークスの製造方法において必
須のチャーの製造を説明する概略図である。Embodiments of the Invention Hereinafter, the method of the present invention will be described in detail with reference to the drawings.
FIG. 1 is a schematic diagram illustrating the production of essential char in the method of producing coke according to the present invention.
第1図に示すように、所定粒度に粉砕された原料の低
炭化度炭を、石炭フィーダー(1)を用いて一定の供給
速度で竪型の管型流通式の反応器(3)に送り込んでや
る。他方、所定温度まで昇温されたキャリヤーガスも同
時に反応器へ送られ、ここで原料炭と高温のキャリヤー
ガスとが接触し、原料炭は極めて短時間で昇温され、熱
分解する。熱分解生成物中の固形分のチャーは、チャー
受器(7)に残渣として捕集され、ガス及びタール蒸気
等は、次の冷却トラップ(8)を通過し、冷却され、タ
ール等の液状生成物は、この冷却トラップ(8)に集め
られ、ガスだけが系外にブロワー(10)によって排出さ
れる。本発明に係るコークスの製造方法は、このように
して得られたチャーを、通常の原料炭への配合用炭材と
し、通常のコークス炉で乾留して高反応性コークスを得
る方法である。As shown in FIG. 1, raw material low-carbon coal pulverized to a predetermined particle size is fed into a vertical tubular flow reactor (3) at a constant feed rate using a coal feeder (1). Do it. On the other hand, the carrier gas heated to a predetermined temperature is also sent to the reactor at the same time, where the raw coal and the high-temperature carrier gas come into contact, and the raw coal is heated in a very short time and thermally decomposed. The solid char in the pyrolysis product is collected as a residue in a char receiver (7), and the gas and tar vapor pass through the next cooling trap (8) and are cooled to form a liquid such as tar. The product is collected in the cooling trap (8), and only gas is discharged out of the system by the blower (10). The method for producing coke according to the present invention is a method in which the char thus obtained is used as a carbon material for blending into ordinary coking coal, and carbonized in an ordinary coke oven to obtain highly reactive coke.
次に、本発明の方法において必須のチャーの製造条件
について、さらに具体的に説明する。Next, the production conditions of the essential char in the method of the present invention will be described more specifically.
チャーを製造する原料石炭の低炭化度炭としては、低
石炭化度の弱粘結炭又は非粘結炭等の低品位炭(褐炭、
亜歴青炭)を使用することができる。又、石炭粒径とし
ては、3mm以下のものが80%程度以下であれば良いが、
望ましくは35メッシュ以下程度の粒径の石炭が用いられ
る。Low-rank coal such as weakly-coking coal or non-coking coal with a low degree of coalification, such as lignite,
Subbituminous coal) can be used. In addition, the coal particle size may be about 3% or less and about 80% or less,
Desirably, coal having a particle size of about 35 mesh or less is used.
かかる原料石炭の熱分解については、石炭の種類にも
よるが、約650℃付近からC−C結合の開裂が激しくな
り、炭化水素ガス、液状生成物の収率が増大する。又、
850℃程度をこえると、一旦生成した分子量の大きいラ
ジカル成分の重縮合によるチャーへの転換が激しくなる
ため、炭素の液状生成物への転化率が再び低下し始め
る。従って、上記原料石炭を急速熱分解させる反応温度
としては、600〜1000℃、望ましくは650〜850℃程度が
適当である。Regarding the thermal decomposition of such raw coal, although it depends on the type of coal, the C—C bond is severely cleaved from about 650 ° C., and the yield of hydrocarbon gas and liquid products increases. or,
When the temperature exceeds about 850 ° C., the conversion of the once generated radical component having a high molecular weight to char by virtue of polycondensation becomes severe, and the conversion of carbon into a liquid product starts to decrease again. Therefore, the reaction temperature for rapidly pyrolyzing the raw material coal is 600 to 1000 ° C, preferably about 650 to 850 ° C.
急速熱分解の反応時間は、温度、滞留時間等によって
昇温速度が変化するために一義的には決定しにくいが、
10秒以下程度で、石炭の昇温速度は、数度〜106℃/秒
程度の急速加熱が適当である。The reaction time of rapid pyrolysis is difficult to determine uniquely because the temperature rise rate changes depending on temperature, residence time, etc.
In about 10 seconds or less, the heating rate of the coal is suitable for rapid heating of several degrees to about 10 6 ° C / second.
また、上記の原料石炭のキャリヤーガスとしては、窒
素、アルゴン、燃焼排ガス等の不活性ガス、あるいは、
水素、メタン、コークス炉ガス等の活性ガスが用いら
れ、キャリヤーガスの温度は、600〜1000℃程度が適当
である。Further, as the carrier gas of the raw material coal, nitrogen, argon, an inert gas such as combustion exhaust gas, or
An active gas such as hydrogen, methane, or coke oven gas is used, and the temperature of the carrier gas is suitably about 600 to 1000 ° C.
[実施例] 次に、本発明を実施例により更に具体的に説明する。
例中、「%」は特に断らない限り「重量%」である。EXAMPLES Next, the present invention will be described more specifically with reference to examples.
In the examples, "%" is "% by weight" unless otherwise specified.
また、コークス類の性状の中、特に重要な回転強度と
反応性につき、JIS K2151の規定により、下記のように
して試験を行った。In addition, among properties of cokes, particularly important rotational strength and reactivity were tested as follows in accordance with JIS K2151.
(1)回転強度(ドラム試験による): ドラムは厚さ9mm、内径150mm、長さ150mmで、内面に
厚さ9mm、幅250mmの羽根が6枚垂直に固定されている。
このドラムに50mm以上の塊コークス10kgを入れて15rpm
で150回転させたのち、50mm、25mm、15mm目ふるいでそ
れぞれふるい分け、ふるい上重量の試料に対する百分率
で、その回転数に対する強度をあらわす。この場合には
▲DI150 15▼として表示する。(1) Rotational strength (according to a drum test): The drum has a thickness of 9 mm, an inner diameter of 150 mm, and a length of 150 mm, and six blades of 9 mm in thickness and 250 mm in width are vertically fixed on the inner surface.
Put 10kg of lump coke of 50mm or more into this drum and 15rpm
And then sieve through 50 mm, 25 mm, and 15 mm sieves respectively, and express the strength with respect to the number of rotations as a percentage of the weight on the sieve relative to the sample. In this case, it is displayed as ▲ DI 150 15 ▼.
(2)反応性: 試料として840〜1680μmの粉コークスを950℃に保っ
た反応管中に規定の高さに充てんする。ここに炭酸ガス
を50cc/minの流速で通じ、未反応の炭酸ガスを苛性カリ
溶液で吸収、除去して、生成した一酸化炭素の流速を求
め、一分間の流量m1をもって反応性指数とする。(2) Reactivity: Fill 840 to 1680 μm coke flour as a sample into a reaction tube maintained at 950 ° C. to a specified height. Here, carbon dioxide gas is passed at a flow rate of 50 cc / min, and unreacted carbon dioxide gas is absorbed and removed with a caustic potash solution, the flow rate of the generated carbon monoxide is determined, and the flow rate m1 per minute is defined as the reactivity index.
[実施例1〜実施例2] 低炭化度炭の弱粘結炭(豪州産、揮発分36%)を原料
とし、キャリヤーガスとして流速10/minの窒素ガスを
使用し、反応温度約850℃、反応時間0.3秒で急速熱分解
して残渣のチャーを得た。その性状は、後記第1表に示
したとおりである。[Examples 1 and 2] Nitrogen gas at a flow rate of 10 / min was used as a carrier gas from a low-carbon coal weakly caking coal (produced in Australia, volatile matter: 36%) at a reaction temperature of about 850 ° C. A rapid pyrolysis was performed with a reaction time of 0.3 seconds to obtain a residue char. Its properties are as shown in Table 1 below.
次に、後記第1表に示す性状のグーニエラ炭(豪州産
の強粘結炭)を原料とし、低炭化度炭の急速熱分解によ
って得られた上記のチャーを原料炭への配合用炭材と
し、後記第3表に示す割合で該グーニエラ炭に配合した
ものを試験炉(装入量15g)に装入して、後記第2表に
示す罐焼条件によりコークスを製造した。得られたコー
クスの性状を、後記第3表にまとめて示した。Next, the above char obtained by the rapid pyrolysis of low-carbon coal is used as a raw material from the Gouniera coal (strongly caking coal produced in Australia) having the properties shown in Table 1 below. A mixture mixed with the Gunniera coal at the ratios shown in Table 3 below was charged into a test furnace (charge amount 15 g), and coke was produced under canning conditions shown in Table 2 below. The properties of the obtained coke are shown in Table 3 below.
[比較例1〜比較例3] グーニエラ炭単独(比較例1)及びグーニエラ炭の通
常のコークスブリーズ(性条は後記第1表参照)を配合
したもの(比較例2,3)のそれぞれを上記の試験炉に装
入して、後記第2表の罐焼条件によりコークスを製造し
た。得られたコークスの性状を、後記第3表にまとめて
比較表示した。[Comparative Examples 1 to 3] Each of the Gunniera charcoal alone (Comparative Example 1) and a mixture of Gunniera charcoal breathing coke breathes (see Table 1 below for the properties) (Comparative Examples 2 and 3) were used. , And coke was manufactured under the baking conditions shown in Table 2 below. The properties of the obtained coke are summarized and shown in Table 3 below.
上記第3表から、本発明方法で得られた実施例のコー
クスは、比較例で得られた従来のコークスに比べ、回転
強度は何ら遜色がなく、しかも反応性は格段に優れてい
ることが判る。 From Table 3 above, it can be seen that the coke of the example obtained by the method of the present invention has the same rotational strength as that of the conventional coke obtained in the comparative example, and has much higher reactivity. I understand.
[発明の効果] 以上詳記したように、本発明方法によれば、低炭化度
炭を原料とし急速熱分解によって得られるチャーをコー
クス製造の原料炭に配合することによって、強度と塊度
とが損なわれることがなく、優れた反応性(反応性指数
17以上)を発揮するコークスを容易に製造することがで
き、この工業的利用価値は極めて大である。[Effects of the Invention] As described in detail above, according to the method of the present invention, the charcoal obtained by rapid pyrolysis using low-carbon coal as a raw material is blended into the raw coal for coke production, whereby strength and bulkiness are improved. Excellent reactivity (reactivity index
(17 or more) can be easily produced, and its industrial utility value is extremely large.
第1図は本発明の方法において用いるチャーの製造を説
明する概略図である。 1……石炭フィーダー、2……キャリヤーガス予熱炉、
3……反応器、4……反応炉、5……キャリヤーガス流
量計、6……差圧計、7……チャー受器、8……液状生
成物補集器(冷却トラップ)、9……ガスサンプラー、
10……ブロワー、11……ガスメーターFIG. 1 is a schematic diagram illustrating the production of a char used in the method of the present invention. 1 ... Coal feeder, 2 ... Carrier gas preheating furnace,
3 ... Reactor, 4 ... Reactor, 5 ... Carrier gas flow meter, 6 ... Differential pressure gauge, 7 ... Char receiver, 8 ... Liquid product collector (cooling trap), 9 ... Gas sampler,
10 …… Blower, 11… Gas meter
───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 昭52−112602(JP,A) 特開 昭54−141802(JP,A) 特開 昭54−112901(JP,A) 特開 昭56−136882(JP,A) (58)調査した分野(Int.Cl.6,DB名) C10B 57/04──────────────────────────────────────────────────続 き Continuation of front page (56) References JP-A-52-112602 (JP, A) JP-A-54-141802 (JP, A) JP-A-54-112901 (JP, A) JP-A-56-112 136882 (JP, A) (58) Field surveyed (Int. Cl. 6 , DB name) C10B 57/04
Claims (1)
0℃、反応時間10秒以下の条件下で急速熱分解によって
得られるチャーを、コークスを製造する際の原料炭への
配合用炭材として使用することを特徴とする高反応性コ
ークスの製造方法。1. A low carbonized coal is used as a raw material and has a reaction temperature of 600 to 100.
A method for producing highly reactive coke, comprising using a char obtained by rapid pyrolysis under the conditions of 0 ° C. and a reaction time of 10 seconds or less as a carbon material for blending into raw coal when producing coke. .
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63271490A JP2759326B2 (en) | 1988-10-27 | 1988-10-27 | Coke production method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63271490A JP2759326B2 (en) | 1988-10-27 | 1988-10-27 | Coke production method |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH02117991A JPH02117991A (en) | 1990-05-02 |
JP2759326B2 true JP2759326B2 (en) | 1998-05-28 |
Family
ID=17500777
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63271490A Expired - Lifetime JP2759326B2 (en) | 1988-10-27 | 1988-10-27 | Coke production method |
Country Status (1)
Country | Link |
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JP (1) | JP2759326B2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103740392A (en) * | 2014-01-22 | 2014-04-23 | 安徽工业大学 | Method for rotating disc type continuous heat treatment of low-order weakly caking coal or low-order non-caking coal |
CN104152162A (en) * | 2014-08-01 | 2014-11-19 | 神华集团有限责任公司 | Pyrolysis system for pyrolysis of broken coal, and device and method for producing semicoke, tar and coal gas by pyrolysis of broken coal |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5412940B2 (en) * | 2009-04-28 | 2014-02-12 | 新日鐵住金株式会社 | Method for producing a coagulation material for sinter production |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS52112602A (en) * | 1976-03-19 | 1977-09-21 | Sumitomo Metal Ind Ltd | Compounding ingredients for coke for blasting furnaces and preparation of same |
JPS54112901A (en) * | 1978-02-23 | 1979-09-04 | Sumitomo Metal Ind Ltd | Production of metallurgical coke |
JPS54141802A (en) * | 1978-04-26 | 1979-11-05 | Nippon Kokan Kk <Nkk> | Production of metallurgical coke from non-caking coal having high volatility |
JPS56136882A (en) * | 1980-03-31 | 1981-10-26 | Nippon Kokan Kk <Nkk> | Preparation of char as raw material for metallurgical coke |
-
1988
- 1988-10-27 JP JP63271490A patent/JP2759326B2/en not_active Expired - Lifetime
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103740392A (en) * | 2014-01-22 | 2014-04-23 | 安徽工业大学 | Method for rotating disc type continuous heat treatment of low-order weakly caking coal or low-order non-caking coal |
CN103740392B (en) * | 2014-01-22 | 2015-08-05 | 安徽工业大学 | The method of rotating disc type continuous heat treatment low order weakly caking coal or low order non-caking coal |
CN104152162A (en) * | 2014-08-01 | 2014-11-19 | 神华集团有限责任公司 | Pyrolysis system for pyrolysis of broken coal, and device and method for producing semicoke, tar and coal gas by pyrolysis of broken coal |
Also Published As
Publication number | Publication date |
---|---|
JPH02117991A (en) | 1990-05-02 |
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